A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6058334



Internal ID21967569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:44188558..44188558hg38UCSC Ensembl
chr2:44415697..44415697hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527620
Samples
Known GenesPPM1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6058334
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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